D4T or Abacavir Plus Vitamin Enhancement in HIV-Infected Patients (DAVE)
Status:
Completed
Trial end date:
2006-08-01
Target enrollment:
Participant gender:
Summary
The purpose of this study is to determine the best way to treat people on d4T (stavudine)
with high levels of lactic acid. Switching from d4T to abacavir will be assessed. Adding
riboflavin and thiamine will also be assessed.
Participants will be randomly assigned to one of four groups:
- Group 1 participants will continue to take d4T as part of their antiretroviral (ARV)
regimen, and will be given the vitamin supplements
- Group 2 will continue to take d4T without vitamin supplements
- Group 3 will switch from d4T to abacavir and receive the vitamins
- Group 4 will switch from d4T to abacavir without vitamin supplements.
The study plans to involve eighty participants from Canada and Argentina for a treatment
period of 16 weeks and a follow-up visit at week 24.